OncoMatch/Clinical Trials/NCT07090148
Trial of pTVG-HP+Nivo+Targeted Ablation of Resistant Lesions in Non-Castrate RecurrentOMPC
Is NCT07090148 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies multiple treatments including pTVG-HP DNA vaccine and Anti-PD-1 monoclonal antibody for prostate cancer patients.
Treatment: pTVG-HP DNA vaccine · Anti-PD-1 monoclonal antibody — The goal of this clinical trial is to learn whether an experimental vaccine called pTVG-HP ("vaccine" or "DNA vaccine"), combined with a drug called nivolumab can increase the cancer-fighting ability of a person's immune cells. The main question it aims to answer is whether the combination of medicines can get rid of metastatic tumors in participants with non-castrate, recurrent, oligometastatic prostate cancer. Participants will undergo: * Treatment with pTVG-HP * Treatment with Nivolumab * Radiation Therapy
Check if I qualifyExtracted eligibility criteria
Cancer type
Prostate Cancer
Performance status
ECOG 0–1(Restricted strenuous activity)
Prior therapy
Must have received: radical prostatectomy
Participants must have undergone radical prostatectomy
Must have received: local therapy (surgery and any adjuvant/salvage radiation therapy)
Participants must have completed local therapy by surgery, and any adjuvant/salvage radiation therapy (if required), at least 3 months prior to entry
Cannot have received: LHRH agonist or nonsteroidal antiandrogen
Exception: Neoadjuvant/adjuvant androgen deprivation therapy with radiation or at prostatectomy is acceptable if no PSA progression and ≤24 months duration
Prior treatment with an LHRH agonist or nonsteroidal antiandrogen, except in the following circumstances: Neoadjuvant/adjuvant androgen deprivation therapy administered with radiation therapy or at the time of prostatectomy is acceptable, provided that there was no evidence of PSA progression while on treatment. In this situation, patients must not have received more than 24 months of androgen deprivation treatment. Other treatment with androgen deprivation therapy is prohibited.
Cannot have received: immunosuppressive therapy (chemotherapy or chronic corticosteroids >10 mg prednisone/day)
Participants cannot have evidence of immunosuppression or have been treated with immunosuppressive therapy, such as chemotherapy or chronic treatment dose corticosteroids (greater than the equivalent of 10 mg prednisone per day), within 3 months of the first vaccination.
Cannot have received: other potential or experimental therapies for prostate cancer
Participants previously treated with other potential or experimental therapies for prostate cancer must have discontinued these treatments and completed at least a 4 week washout prior to beginning treatment.
Lab requirements
Blood counts
normal hematologic function
Kidney function
normal renal function
Liver function
normal liver function
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- University of Wisconsin - Madison · Madison, Wisconsin
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